Canonical Allele Identifier: CA668643336

Gene: RPS24

Linked Data

• dbSNP Id: rs1397985222
• gnomAD v3: 10-78036887-TTGGTA-T
• gnomAD v4: 10-78036887-TTGGTA-T
• MyVariant Identifiers: chr10:g.79796646_79796650del (hg19) ; chr10:g.78036888_78036892del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.78036888_78036892del , CM000672.2:g.78036888_78036892del	GRCh38
NC_000010.10:g.79796646_79796650del , CM000672.1:g.79796646_79796650del	GRCh37
NC_000010.9:g.79466652_79466656del	NCBI36
NG_012633.1:g.8129_8133del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360830.9:c.280-306_280-302del	ENSP00000354074.5:n.280-306_280-302del
ENST00000372360.9:c.280-306_280-302del MANE Select	ENSP00000361435.4:n.280-306_280-302del
ENST00000440692.6:c.280-306_280-302del	ENSP00000414321.1:n.280-306_280-302del
ENST00000464716.6:c.280-306_280-302del	ENSP00000494231.1:n.280-306_280-302del
ENST00000465692.2:n.291-306_291-302del
ENST00000475468.6:n.690-306_690-302del
ENST00000476545.6:c.280-306_280-302del	ENSP00000494169.1:n.280-306_280-302del
ENST00000478655.6:n.319-306_319-302del
ENST00000485708.7:n.319-306_319-302del
ENST00000613865.5:c.280-306_280-302del	ENSP00000478869.2:n.280-306_280-302del
ENST00000645195.1:c.156-306_156-302del
ENST00000645440.1:c.280-306_280-302del	ENSP00000496738.1:n.280-306_280-302del
ENST00000645698.1:n.308-306_308-302del
ENST00000360830.8:c.280-306_280-302del	ENSP00000354074.4:n.280-306_280-302del
ENST00000372360.7:c.280-306_280-302del	ENSP00000361435.3:n.280-306_280-302del
ENST00000435275.5:c.280-306_280-302del	ENSP00000415549.1:n.280-306_280-302del
ENST00000440692.5:c.280-306_280-302del	ENSP00000414321.1:n.280-306_280-302del
ENST00000464716.5:n.308-306_308-302del
ENST00000465692.1:n.277-306_277-302del
ENST00000476545.5:n.304-306_304-302del
ENST00000478655.5:n.319-306_319-302del
ENST00000482069.5:n.347-306_347-302del
ENST00000485708.6:n.338-306_338-302del
ENST00000613865.4:c.280-306_280-302del	ENSP00000478869.1:n.280-306_280-302del
NM_001026.4:c.280-306_280-302del	NP_001017.1:n.280-306_280-302del
NM_001142282.1:c.280-306_280-302del	NP_001135754.1:n.280-306_280-302del
NM_001142283.1:c.280-306_280-302del	NP_001135755.1:n.280-306_280-302del
NM_001142284.1:c.280-306_280-302del	NP_001135756.1:n.280-306_280-302del
NM_001142285.1:c.280-306_280-302del	NP_001135757.1:n.280-306_280-302del
NM_033022.3:c.280-306_280-302del	NP_148982.1:n.280-306_280-302del
XM_011540034.1:c.433-306_433-302del	XP_011538336.1:n.433-306_433-302del
XM_011540035.1:c.433-306_433-302del	XP_011538337.1:n.433-306_433-302del
XM_011540036.1:c.433-306_433-302del	XP_011538338.1:n.433-306_433-302del
XM_011540037.1:c.433-306_433-302del	XP_011538339.1:n.433-306_433-302del
XM_011540038.1:c.433-306_433-302del	XP_011538340.1:n.433-306_433-302del
NM_001142285.2:c.280-306_280-302del	NP_001135757.1:n.280-306_280-302del
NM_033022.4:c.280-306_280-302del MANE Select	NP_148982.1:n.280-306_280-302del
NM_001026.5:c.280-306_280-302del	NP_001017.1:n.280-306_280-302del
NM_001142282.2:c.280-306_280-302del	NP_001135754.1:n.280-306_280-302del
NM_001142283.2:c.280-306_280-302del	NP_001135755.1:n.280-306_280-302del
NM_001142284.2:c.280-306_280-302del	NP_001135756.1:n.280-306_280-302del